WO1997004947A1 - Pressure sensitive adhesive patch - Google Patents
Pressure sensitive adhesive patch Download PDFInfo
- Publication number
- WO1997004947A1 WO1997004947A1 PCT/US1995/009467 US9509467W WO9704947A1 WO 1997004947 A1 WO1997004947 A1 WO 1997004947A1 US 9509467 W US9509467 W US 9509467W WO 9704947 A1 WO9704947 A1 WO 9704947A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- patch
- backing
- pressure sensitive
- sensitive adhesive
- article
- Prior art date
Links
- 239000004820 Pressure-sensitive adhesive Substances 0.000 title claims abstract description 67
- 239000010410 layer Substances 0.000 claims abstract description 47
- 239000000758 substrate Substances 0.000 claims abstract description 19
- 230000003068 static effect Effects 0.000 claims abstract description 13
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 12
- 239000010935 stainless steel Substances 0.000 claims abstract description 12
- 239000000853 adhesive Substances 0.000 claims description 57
- 230000001070 adhesive effect Effects 0.000 claims description 57
- 239000000463 material Substances 0.000 claims description 54
- 238000011084 recovery Methods 0.000 claims description 32
- 229920000098 polyolefin Polymers 0.000 claims description 11
- 229920001684 low density polyethylene Polymers 0.000 claims description 9
- 239000004702 low-density polyethylene Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 229920002635 polyurethane Polymers 0.000 claims description 9
- 239000004814 polyurethane Substances 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- 230000007547 defect Effects 0.000 claims description 8
- 229920001296 polysiloxane Polymers 0.000 claims description 8
- 229920001400 block copolymer Polymers 0.000 claims description 7
- 229920000728 polyester Polymers 0.000 claims description 7
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 claims description 3
- 229920000092 linear low density polyethylene Polymers 0.000 claims 2
- 239000004707 linear low-density polyethylene Substances 0.000 claims 2
- 238000012360 testing method Methods 0.000 description 29
- 229920001971 elastomer Polymers 0.000 description 16
- 239000002904 solvent Substances 0.000 description 13
- -1 polyethylene Polymers 0.000 description 12
- 239000005060 rubber Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 9
- 229920000573 polyethylene Polymers 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 8
- 239000002131 composite material Substances 0.000 description 7
- 229920000359 diblock copolymer Polymers 0.000 description 7
- 150000001993 dienes Chemical class 0.000 description 7
- 230000008439 repair process Effects 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 5
- 239000000806 elastomer Substances 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229920002633 Kraton (polymer) Polymers 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- 239000003082 abrasive agent Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000012790 adhesive layer Substances 0.000 description 4
- 229920005549 butyl rubber Polymers 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920001084 poly(chloroprene) Polymers 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000013013 elastic material Substances 0.000 description 3
- 238000005188 flotation Methods 0.000 description 3
- 239000002655 kraft paper Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920001875 Ebonite Polymers 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920006266 Vinyl film Polymers 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- GAODDBNJCKQQDY-UHFFFAOYSA-N 2-methyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCC)=C1 GAODDBNJCKQQDY-UHFFFAOYSA-N 0.000 description 1
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 1
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 229920013665 Ampacet Polymers 0.000 description 1
- 241001120493 Arene Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 241000545744 Hirudinea Species 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
- 229920013623 Solprene Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000006664 bond formation reaction Methods 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000004482 other powder Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000000807 solvent casting Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229920000428 triblock copolymer Polymers 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C73/00—Repairing of articles made from plastics or substances in a plastic state, e.g. of articles shaped or produced by using techniques covered by this subclass or subclass B29D
- B29C73/04—Repairing of articles made from plastics or substances in a plastic state, e.g. of articles shaped or produced by using techniques covered by this subclass or subclass B29D using preformed elements
- B29C73/10—Repairing of articles made from plastics or substances in a plastic state, e.g. of articles shaped or produced by using techniques covered by this subclass or subclass B29D using preformed elements using patches sealing on the surface of the article
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2021/00—Use of unspecified rubbers as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2030/00—Pneumatic or solid tyres or parts thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T152/00—Resilient tires and wheels
- Y10T152/10—Tires, resilient
- Y10T152/10882—Patches
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/20—Patched hole or depression
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
- Y10T428/2896—Adhesive compositions including nitrogen containing condensation polymer [e.g., polyurethane, polyisocyanate, etc.]
Definitions
- the present invention relates to repair patches, particularly pressure sensitive repair patches for inflatable articles such as bicycle inner tubes, beach toys, personal flotation devices, and the like.
- the solvent-based adhesive patching system typically consists of a relatively thick patch typically about 1.3 mm and a container of a solvent-based adhesive. This system is used to repair an inner tube by first cleaning and/or abrading the punctured area, applying the solvent-based adhesive, allowing the solvent to evaporate, applying the patch, and waiting 15-20 minutes before pressurizing the inner tube.
- the patch is typically made from a rubber such as neoprene rubber.
- a similar system includes a two-layer patch having a main body of vulcanized rubber and a thin layer of nonvulcanized rubber adhered thereto, and a container of a vulcanizing fluid or "cement."
- the "adhesive" is formed when the layer of nonvulcanized rubber is contacted with the vulcanizing fluid that reacts with the uncombined sulfur to fully cure the rubber.
- the pressure sensitive patching system typically consists of a single- sided pressure sensitive patch that can be approximately 0.75-1.5 mm thick.
- patches typically have a thick backing and a thin layer of pressure sensitive adhesive disposed on one side of the backing.
- the backings are typically at least about 0.75 mm thick and the adhesive layers are typically about 0.05 mm thick.
- the backings are typically made of opaque polyethylene foam or thick neoprene rubber.
- the adhesives are typically rubber-based or acrylic pressure sensitive adhesives.
- the thick patch is applied over a hole in an inner tube, for example, after abrading or cleaning the punctured area to remove talc or other powder from the inner tube. Because this patch is pressure sensitive, it overcomes the inconvenience and time consuming weaknesses of the solvent-based adhesive patch system.
- the present invention provides a patch that includes a backing and a pressure sensitive adhesive layer having an average thickness of greater than about 0.076 mm disposed on the backing.
- the patch has a maximum thickness of no greater than about 0.64 mm, a T-Peel strength from an organic polymeric substrate of at least about 0.18 kN/m after 1 hour dwell time at 22°C, and a static shear strength of at least about 50 minutes from stainless steel at 70°C with a 7.6 kPa load.
- the patch can be used on a wide variety of articles that need a defect, such as a hole or puncture, repaired.
- the patch is particularly useful for patching inflatable articles such as bicycle inner tubes, beach toys, personal flotation devices, beds, boats, air mattresses, balloons, the amusement park entertainment device referred to as the "moon walk," and other inflatable amusement devices.
- the present invention also provides a hollow inflatable article having the patch described above adhered thereto.
- the present invention also provides a kit for repairing an article, particularly an inflatable article such as a bicycle inner tube.
- the kit includes the patch described above; surface preparation means; and instructions for applying the patch to an article to be repaired.
- the surface preparation means can be an abrasive material, a solvent-soaked pad such as an alcohol-soaked pad, or the like.
- the present invention provides a method of repairing an article. The method includes the step of applying the patch described above over a defect, e.g., hole, in the wall ofthe article.
- Figure 1 is a side view of a patch ofthe invention.
- Figure 2 is a plan view ofthe patch shown in Figure 1, partially cut away, disposed on a release liner.
- Figure 3 is a bicycle inner tube with the patch of Figure 1 adhered thereto.
- the present invention provides a patch, a kit, and a method for repairing a variety of organic polymeric articles, such as rubber or plastic articles.
- the patch and kit are particularly suitable for patching inflatable articles, such as inner tubes for bicycle and tractor tires, rubber balls, water toys, boats, air mattresses, balloons, personal flotation devices, the amusement park entertainment device commonly referred to as the "moon walk", and other inflatable vinyl or rubber items, for example.
- inflatable articles such as inner tubes for bicycle and tractor tires, rubber balls, water toys, boats, air mattresses, balloons, personal flotation devices, the amusement park entertainment device commonly referred to as the "moon walk", and other inflatable vinyl or rubber items, for example.
- the invention is applicable to any type of article that needs to be repaired to keep air or water, for example, from passing through a defect in the wall ofthe article.
- the adhesive for applying the patch to an article is a pressure sensitive adhesive. It is disposed on one surface of a backing. Thus, the patch does not require the user to apply glue. Therefore, the patch ofthe present invention can be easily applied to an article to repair a defect such as a hole or puncture. It is a simple, fast, and convenient method of repairing a bicycle inner tube, for example.
- the patch ofthe present invention is generally less sensitive to "user error" than are conventional pressure sensitive adhesive patches. Reduced user error or user sensitivity typically results, for example, if the patch has good adhesion substantially immediately upon application.
- the patch of the present invention is particularly advantageous because it is very thin, compared to most conventional patches. This contributes to reduced user sensitivity as thin patches have less of a tendency to slip.
- the patch has a maximum thickness of no greater than about 0.64 mm, preferably no greater than about 0.50 mm, more preferably no greater than about 0.40 mm, and most preferably no greater than about 0.30 mm.
- This thin profile decreases the amount of wear a tire experiences in the area of the patch.
- the patch can be thicker in the center and thinner at the periphery if desired. At no point along the profile, however, is the patch thicker than about 0.64 mm. This is particularly desirable for patching bicycle tire inner tubes to reduce the amount of localized wear on the tire.
- the patch of the present invention is also particularly advantageous because it adheres well under both high and low temperature conditions (e.g., -18°C to 70°C). Low temperature adhesion is typically important in the application step of the patch, whereas high temperature adhesion is important during use of the patched article to avoid slippage of the patch. Patches can be warmed by hand during application if the temperature is below about 4°C.
- the patch of the present invention uses a thinner backing coupled with a thicker layer of adhesive than commercially available PSA patches.
- the backing preferably has a maximum thickness of no greater than about 0.40 mm, more preferably no greater than about 0.30 mm, and most preferably no greater than about 0.10 mm.
- the backing generally serves as simply a carrier for the adhesive when the patch is held in place by externally applied pressure, i.e., when it is constrained. However, when the patch is unconstrained, the backing thickness is more important to the performance of the patch.
- the backing has a thickness of at least about 0.01 mm, more preferably at least about 0.03 mm, and most preferably at least about 0.05 mm. Again, this is particularly desirable for patching bicycle tire inner tubes to reduce the amount of localized wear on the tire.
- the pressure sensitive adhesive layer preferably has a thickness (average) of greater than about 0.076 mm, more preferably at least about 0.089 mm, and most preferably at least about 0.10 mm.
- a relatively thick layer of a pressure sensitive adhesive is needed for high peel strength; however, the thicker the layer of adhesive, the lower the shear strength.
- the thickness of the adhesive layer is chosen to balance the peel and shear strength values.
- the adhesive layer is no greater than about 0.40 mm thick, and more preferably, no greater than about 0.30 mm thick.
- a thick layer of adhesive has advantages over a thin layer having the same adhesive performance properties because it generally will conform and seal better to a substrate.
- the patch of the present invention has a T-Peel strength of greater than about 0.18 kN/m from an organic polymeric substrate after 1 hour dwell time at 22°C, and a static shear strength of at least about 50 minutes from stainless steel at 70°C with a 7.6 kPa load.
- the patch has a T-Peel strength from an organic polymeric substrate of at least about 0.26 kN/m after 1 hour dwell time at 22°C, and a static shear strength of at least about 100 minutes from stainless steel at 70°C with a 7.6 kPa load.
- the patch has a T-Peel strength from an organic polymeric substrate of at least about 0.35 kN/m after 1 hour dwell time at 22°C, and a static shear strength of at least about 300 minutes on stainless steel at 70°C with a 7.6 kPa load.
- This T-Peel test is an unconstrained test.
- unconstrained means that the patch is not held in place by externally applied pressure
- dwell time means the period of time the patch is in contact with the substrate before being tested.
- the peel strengths listed above result from the appropriate choice of adhesive for the desired substrate. Preferably, these peel strengths are those obtained using an adhesive on a butyl rubber substrate, such as is used in inner tubes.
- the patches of the present invention can typically withstand pressures in an unconstrained mode of up to about 70 kPa whereas in a constrained mode, such as when used on an inner tube in a bicycle tire, the patches of the present invention can withstand pressures of up to about 825 kPa.
- a constrained mode such as when used on an inner tube in a bicycle tire
- the patches of the present invention can withstand pressures of up to about 825 kPa.
- touring bicycle tires experience pressures of about 690-825 kPa.
- mountain bicycle tires experience pressures of about 275-415 kPa.
- the backing is typically made from a material and in a manner that is generally impervious to the adhesive. If, however, the adhesive is not impervious to air, for example, the backing should be made of a material that it is generally impervious to air to avoid leakage from a patched inflated article.
- the backing can be elastic or nonelastic. Preferably, it is elastic. It is also preferably flexible. An elastic and flexible backing make the patch of the present invention particularly useful for patching bicycle inner tubes. This is because the patch stretches as the inner tube stretches.
- the backing is preferably of a material that is sufficiently transparent that a hole in an inner tube can be seen through the patch.
- the backing can be made from a wide variety of materials including organic polymers, thin metals, ceramic materials, fiberglass, etc.
- the backing can be a single layer or a composite of two or more layers of material.
- the composite can include metallized layers, barrier layers, nonwoven layers, polymer layers, paper layers, antistatic layers, primer layers, foam layers, and the like.
- the patch of the present invention includes a backing made from an elastic polymeric material. This is particularly important when the patch is used in an expandable unconstrained application.
- the elastic polymeric material can be any material that can be stretched and then retum towards its original shape and size.
- the elastic polymeric material has a recovery of at least about 50% after being elongated to 100% of its. original length. More preferably, it has a recovery of at least about 65%, and most preferably at least about 80%, when elongated to 100% of its original length.
- the choice of material of the backing is matched to the material ofthe substrate such that their percent recoveries are substantially (i.e., within about 20%) similar. This generally avoids puckering and gapping ofthe patch when the article is deflated.
- This percent recovery can be determined by the test method described below for Percent Recovery. In this test, a sample of the material is elongated 100% of its original length, held under tension for two minutes, and then allowed to relax for two minutes prior to the determination of the amount of recovery. For an inflatable article, this allows for expansion upon inflation.
- the elastic polymeric material is also preferably flexible. That is, a 0.4 mm thick backing material is preferably capable of being bent to a radius of about 0.5 cm at room temperature (20-25°C) without breaking. A flexible material is desirable so that the patch can conform to the article being patched.
- the elastic, preferably flexible, polymeric material can be in the form of a single layer, multiple layers, or a foam.
- Polymers that can be used to prepare the elastic material include polyolefins and polyolefin copolymers such as low density polyethylene, ultra low density polyethylene, low density polyethylene, polyethylene/polypropylene, and polyethylene/polybutylene; polyurethane; polyester; thermoplastic rubber such as ABA block copolymers; plasticized polyvinyl chloride; blends of vinyl acetate and elastomers; and combinations thereof. Mixtures or blends of any plastic or plastic and elastic materials such as polypropylene/polyethylene, polyurethane/polyolefin, polyurethane/polycarbonate, polyurethane/polyester, and the like, can also be used. Laminate materials such as those described in U.S. Patent No.
- 5,354,597 can also be used as the elastic polymeric material as long as they recover towards their original shape upon elongation, preferably as long as they have a percent recovery of at least about 50%, more preferably at least about 65%, and most preferably at least about 80%, when elongated by 100%. Such materials may require prestretching to achieve the desired level of elasticity.
- thermoplastic rubbers such as KRATON G2712X and KRATON G7705, both of which are commercially available from Shell Chemical Co., Houston, TX; low density polyethylene (LDPE) such as Polyethylene 2503.1, which is commercially available from Dow Chemical Co., Midland, MI, as well as PETROTHENE NA 964-085 and the PETROTHENE NA 960 series, all of which are commercially available from Quantum Chemical Corp., Cincinnati, OH; and ultra low density polyethylene (ULDPE).
- LDPE low density polyethylene
- Polyethylene 2503.1 which is commercially available from Dow Chemical Co., Midland, MI
- PETROTHENE NA 964-085 and the PETROTHENE NA 960 series all of which are commercially available from Quantum Chemical Corp., Cincinnati, OH
- ULDPE ultra low density polyethylene
- the backing can be made using any of the several methods of film forming known in the art such as extrusion, coextrusion, solvent casting, and the like.
- the backing can be of any thickness so long as the overall patch thickness is no greater than about 0.64 mm, and the layer of adhesive is sufficiently thick to provide the desired levels of peel and shear strength.
- a thin backing is preferred, but it should be thick enough to provide adequate tensile strength for a particular application and processing method. For example, when the backing is processed, it should be able to withstand the tension produced without tearing.
- the thickness of the backing should also be considered as it relates to the recovery force exerted by the material upon being stretched.
- the recovery force is the force exerted by an elongated strip of material to retum to its natural state.
- the Peak Load test provided below is a measurement of the maximum recovery force exhibited by a strip of material elongated to 100% of its original state.
- the recovery force increases relative to the thickness of the material.
- the thickness of the material may be selected to provide an appropriate level of recovery force. It is desirable that the recovery force remaining upon bond formation and partial recovery of the elastic material be low to prevent failure ofthe bond. High recovery forces can cause premature peel mode failures in expandable unconstrained applications and shear mode failure in constrained applications.
- the material and thickness of the backing are chosen such that the peak load recovery force measured at 100% elongation is less than the strength of the bond formed between the patch and the article to prevent failure in the peel and or shear mode.
- the recovery force of a backing material is less than about 2.5 kN/m, more preferably less than about 1.8 kN/m, and most preferably less than about 0.9 kN/m.
- Particularly preferred patches ofthe present invention include a backing having a recovery force of less than about 0.18 kN/m.
- the recovery force appears to be directly proportional to the thickness of the backing, at least for some materials.
- the Peak Load was measured for a material made from PETROTHENE NA 964-085 with 4 wt-% REMAFIN Blue AEW U-18 colorant for three different thicknesses (0.073 mm, 0.58 kg/cm; 0.095 mm, 0.83 kg/cm; 0.12 mm, 1.00 kg/cm).
- the Peak Load per unit length increased proportionately with the material thickness, so that the Peak Load per unit area remained relatively constant (170 kg/cm 2 , 190 kg/cm 2 , and 180 kg/cm , respectively).
- a suitable material thickness may be selected to provide a recovery force that is appropriate for a particular application based on adhesive performance.
- the backing can contain additives such as colorants, antioxidants, antistatic agents, fillers, particulates, and the like. Ideally, no colorants, fillers, or particulates are incorporated into the backing, particularly if they produce an opaque patch; antioxidants are generally desirable, however. A patch that is sufficiently transparent or clear to see the hole and adhesive wet out is desirable for easy center placement over a hole. Furthermore, additives such as fillers can reduce the elasticity ofthe backing. Thus, if used, the additives are used in an amount such that they do not substantially affect the bond performance or elastic properties of the patch.
- colorants e.g., pigments and dyes
- colorants include REMAFIN Blue AEW U-18, which is commercially available from Resco Colors, a subsidiary of Hoechst Canada Inc., Mississauga, Ontario, and No. 16180 Dark Blue Color Concentrate, which is commercially available from Ampacet, Tarrytown, NY.
- antioxidants include IRGANOX 1520 and IRGANOX 1010, both of which are commercially available from Ciba Geigy, Mclntosh, TX.
- fillers include calcium carbonate, carbon black, glass beads, polymeric and glass bubbles, short fibers of glass or nylon, silica, magnesium oxide, and talc.
- particulates include thermally conductive particulates and microwave susceptors.
- each additive is preferably present in an amount less than about 20 percent by weight (wt-%), based on the total weight ofthe backing material. More preferably, when used antioxidants are present in an amount of less than about 2 wt- %, and colorants are present in an amount of less than about 10 wt-%.
- wt-% percent by weight
- Pressure sensitive adhesives are a standard class of materials. They have a four-fold balance of adhesion, cohesion, stretchiness, and elasticity. They have an open time tack (i.e., period of time during which the adhesive is tacky at room temperature (i.e., about 20-25°C)) on the order of days and often months or years and firmly adhere to a variety of dissimilar surfaces upon contact. They require no activation by water, solvent, or heat in order to exert a strong adhesive holding force toward such materials as paper, cellophane, glass, plastic, wood, and metals. Typically, pressure sensitive adhesives have a sufficient cohesive strength and elastic properties such that, despite their aggressive tackiness, they can be handled with the fingers and removed from smooth surfaces without leaving a substantial residue.
- Pressure sensitive adhesives suitable for use in this invention are coatable adhesives.
- a wide variety of coatable pressure sensitive adhesives can be used, such as solvent coatable, hot melt coatable, as well as latex PSA's that are coatable out of water.
- solventless curable adhesives (often referred to as 100% solids) can be used. Where thicker adhesive coatings are desired, it may be desirable either to apply multiple layers of the adhesive, hot melt coat, or to photopolymerize the adhesive m sjtu.
- Specific examples of pressure sensitive adhesives include acrylates, such as isooctyl acrylate/acrylic acid copolymers, tackified acrylates, and plasticizer-containing acrylates such as those disclosed in U.S. Patent No.
- 4,946,742 (Landin); natural or synthetic rubber resins, including thermoset rubbers as well as thermoplastic rubbers and elastomers, such as nitrile rubbers (e.g:, acrylonitrile-butadiene), styrene-butadiene, styrene-isoprene, styrene- butadiene-styrene, styrene-isoprene-styrene, and natural rubber; silicone-based adhesives, such as polysiloxanes; polyolefins; polyesters; polyamides; and polyurethanes.
- nitrile rubbers e.g:, acrylonitrile-butadiene
- styrene-butadiene styrene-isoprene
- styrene-butadiene-butadiene-styrene-isoprene styrene-butadiene-
- the pressure sensitive adhesive suitable for use in the present invention can be any desired adhesive that is capable of adhering to the article to be repaired.
- the specific composition of the pressure sensitive adhesive is irrelevant to the present invention as long as the PSA meets the other characteristics described herein.
- it is an adhesive that will adhere to the materials used to prepare inflatable articles, such as vinyls, butyl rubber, neoprene, and the like.
- One of skill in the art can typically match the adhesive to the substrate for effective adhesion.
- the rubber resins and tackified acrylates can be used on butyl rubber and the plasticizer-containing acrylates can be used on vinyls.
- a preferred class of pressure sensitive adhesives are the diblock A-B type and triblock A-B-A or A-B-C type block copolymers, or mixtures thereof, such as those referred to under the tradename KRATON of Shell Oil Company.
- These are polymer blocks wherein A is a thermoplastic polymer block with a glass transition temperature above room temperature and which is relatively incompatible with the elastomeric B segment.
- B and C are typically polymer blocks of a conjugated diene such as butadiene or isoprene. While the conjugated diene employed in the B block may differ from that employed in the C block, it is preferred that the same diene be employed in both blocks. These blocks may be partially or completely hydrogenated. Examples of such diblock and triblock copolymers are disclosed in U.S. Patent Nos. 4,444,953 and 3,239,478.
- a particularly preferred pressure sensitive adhesive comprises an elastomeric phase which is predominantly of diblock A-B type block copolymers wherein the A blocks are of a monoalkenyl aromatic hydrocarbon or a monoalkenyl arene, mainly polystyrene or polystyrene derivatives, having a weight average molecular weight of about 4,000-50,000, preferably about 7,000-30,000, and the B blocks are predominantly 1,3 -butadiene.
- the A block content is about 7-50 wt-% of the block copolymer, preferably about 10-35 wt-%.
- the A block can also be formed predominately of t ⁇ -methylstyrene, t-butylstyrene, and other ring alkylated styrenes, and can also contain minor proportions of other monomers, such as conjugated dienes.
- the B groups have a weight average molecular weight of about 5,000-500,000, preferably about 50,000-300,000. Minor proportions of other monomers can be included in the B blocks, e.g., residue arenes or other conjugated dienes.
- B groups can also contain conjugated dienes other than 1,3- butadiene in amounts up to about 50% by weight ofthe total B blocks.
- A-B type block copolymer elastomers or other conventional elastomers, preferably diene elastomers, can be employed in amounts up to about 75 wt-% (preferably up to about 50 wt-%) ofthe multiblock portion ofthe elastomeric phase.
- the remaining portion ofthe elastomeric phase comprises multiblock A-B, linear (other than diblock), star, radial, or otherwise branched, type block copolymer of the above-described A blocks, and B blocks of conjugated dienes, preferably, 1,3-butadiene.
- This multiblock A-B type block copolymer has there or more blocks, the terminal portion of at least two branches or ends are preferably of A blocks.
- this portion of the elastomeric phase comprises a linear triblock A-B type block copolymer.
- a specific embodiment of this pressure sensitive adhesive is one that includes 100 parts of an elastomeric phase containing about 78-98 parts (preferably about 80-95 parts) of an elastomeric diblock A-B type block copolymer of predominately monoalkenyl arene (preferably polystyrene or polystyrene derivatives) A blocks, and poly-l,3-butadiene B blocks.
- the elastomeric phase also contains about 2-22 parts of a multiblock elastomer portion of the elastomeric phase comprising an A-B type block copolymer of at least 3 blocks, wherein the B block is predominantly 1,3 -butadiene and the A block is predominantly a monoalkenyl arene.
- the elastomeric phase is tackified with a solid tackifying resin (preferably about 80-140 parts per 100 parts elastomeric phase) and an oil or liquid tackifier (preferably about 5-35 parts per 100 parts elastomeric phase) to provide an adhesive having a composite midblock glass transition temperature (CMTg) of less than about -10°C.
- a solid tackifying resin preferably about 80-140 parts per 100 parts elastomeric phase
- an oil or liquid tackifier preferably about 5-35 parts per 100 parts elastomeric phase
- CMTg composite midblock glass transition temperature
- a layer of pressure sensitive adhesive 12 is disposed directly on one surface of a backing 14.
- no primer layer or priming method are necessary to adhere the pressure sensitive adhesive layer 12 to the backing 14, although this could be done if desired for certain combinations of adhesive and backing material.
- a release liner 16 is disposed on the exposed surface 15 of the layer of pressure sensitive adhesive 12.
- the patch 10 is removed from the release liner 16 and the exposed surface 15 of the pressure sensitive adhesive layer is applied to a defect in the article, e.g., a puncture in a bicycle tire inner tube 20 shown in Figure 3. Little preparation ofthe surface of the article is required prior to placement of the patch.
- the surface can be slightly abraded with a piece of abrading material, cleaned with a solvent, or simply wiped with a dry cloth.
- preferred patches ofthe present invention are sufficiently transparent for easy placement of the patch over the defect in the article to be repaired. Furthermore, such clear patches allow the user to see the wet out ofthe relatively thick layer of adhesive over the abraded or cleaned surface.
- the patches of the present invention may also include a release liner to protect the pressure sensitive adhesive during storage or to permit the patches to be formed into a roll or pad.
- Release liners also prevent unintended contact ofthe adhesive with other surfaces.
- Release liners are prepared from release coatings, such as silicone release coatings, deposited on a substrate.
- One of the most common substrate is supercalendared kraft paper.
- Other suitable substrates include coated papers such as polyethylene coated kraft paper, clay coated kraft paper, and glassine paper; and non-porous films such as polyethylene, polypropylene, polyester, and polyethylene terephthalate.
- Useful release coatings can be prepared from any polymer of lower critical surface tension and of different polarity than that of the adhesive.
- the patch of the present invention can be prepared by well known techniques in the art of tape manufacturing. For example, a layer of the adhesive can be applied to the backing material by hot melt coating, solvent coating, extruding, or laminating. This can then be applied to a release liner. Alternatively, the adhesive can be applied to the release liner and then the adhesive-coated release liner can be combined with the backing by laminating. Individual patches can cut in any of a variety of sizes and shapes, such as squares, rectangles, circles, ovals, and the like.
- the patch ofthe present invention is preferably included within a kit containing one or more patches disposed on a release liner.
- the kit further includes surface preparation means, and instructions for repairing an article by applying the patch over a defect in the article, e.g., a hole in the wall of a bicycle inner tube.
- the surface preparation means can be anything appropriate for the desired application. For example, it can be a small piece of a coated abrasive material for preparing the surface of the article. It can be a solvent, e.g., alcohol soaked, pad or cloth. Altematively, it can be simply a small piece of dry cloth.
- the abrasive material and dry cloth are preferred because they can be used repeatedly and will not dry out.
- the dry cloth is more preferred because channels are not formed in the surface of the article through which air could pass if the patch does not conform to the channels. However, if used with light pressure, an abrasive material will not typically form such channels.
- Samples were slit in the down web direction (as opposed from cross web) to a width of 1.3 cm and a length of 20 cm. Samples were marked in the middle with two lines that were 2.5 cm apart. The two lines were perpendicular to the lengthwise dimension ofthe sample. This distance was Ll and denotes the "test area.” Samples were tested using an INSTRON tensile tester (commercially available from Instron Corp., Canton, Massachusetts) with the distance between the jaws set at 5 cm.
- INSTRON tensile tester commercially available from Instron Corp., Canton, Massachusetts
- the sample was clamped in the jaws so that the test area was centered between the upper and lower jaws and elongated in the lengthwise (or machine direction) until the jaws of the INSTRON tensile tester increased the gap by 5 cm, i.e., 100% elongation, at a crosshead speed of about 30 cm/minute.
- the INSTRON tensile tester was stopped at this point and the test sample was held in tension for two minutes. After the two-minute holding period, the tension was removed and the sample was allowed to relax for two minutes. Then the distance between the two lines was remeasured to give stretched length, L2.
- the Percent Recovery was determined by the following equation:
- the desired percent recovery of the backing alone is preferably at least about 50%, more preferably at least about 65%, and most preferably at least about 80%.
- the desired percent recovery of the patch is preferably at least about 50%, more preferably at least about 65%, and most preferably at least about 80%.
- the Peak Load was determined by finding the maximum force value exhibited by a sample during an elongation of 100%. This value was obtained from a recording chart in pounds. This value was then converted to kilograms and divided by the width of the sample to give the Peak Load in kilograms/centimeters (kg/cm). The reported Peak Load was the average of three replicate samples unless otherwise noted.
- Test samples (2.5 cm x 15 cm) included a pressure sensitive adhesive layer on a 0.05 mm thick primed polyester strip. Altematively, commercially available samples were used as is; variations in width were compensated for in the calculations. These were applied to a stainless steel panel or low density polyethylene panel using two passes of a 2 kg hard-rubber roller, one pass in each direction at a rate of about 30 cm/minute. Samples were allowed to dwell for one hour at room temperature (20-25°C) before being separated at a rate of about 30 cm/minute. Two replicates were run and the average value reported.
- a test sample of a pressure sensitive adhesive coated on 0.05 mm thick piece of primed polyester film having the dimensions of 1.3 cm x 15 cm were tested. Altematively, commercially available samples were used as is; variations in width were compensated for in the calculations. Each sample was attached to a 1.6 cm x 15 cm piece of a bicycle inner tube (made from a material containing butyl rubber, SPECIALIZED Product No. 031-1333 24 x 1.5/2.125, made by Specialized, Taiwan. The piece of inner tube was cleaned with methyl ethyl ketone to remove any surface contamination.
- test sample was aligned on top of the inner tube and then pressed together using two passes of a 2 kg hard rubber roller, the roller traveling in opposite directions for each pass at a rate of about 30 cm/minute.
- the test sample was allowed a one-hour dwell at room temperature.
- the two immediately adjacent free ends ofthe sample and inner tube were clamped in the jaws of an INSTRON tensile tester and pulled apart at a crosshead speed of about 30 cm/minute.
- the T-Peel Strength value was reported as the average value over a 2.5-5.0 cm length of test sample. Two replicates were run and the average value reported in kilonewtons/meter (kN/m). This test is an indication of how well an adhesive bonds to a flexible substrate, such as a bicycle inner tube.
- Static shear strength at 70°C was determined as follows: Individual 2.5 cm x 10 cm test samples having a layer of pressure sensitive adhesive on a 0.05 mm thick primed polyester film were bonded to a 5 cm x 13 cm stainless steel panel by passing a 2 kg rubber coated steel roller over the composite two times to form an overlap area of 2.5 cm. Altematively, commercially available samples were used as is; variations in width were compensated for in the calculations. If sample width was less than 2.5 cm wide, then the length was adjusted for a total 6.5 cm 2 overlap area. After about 1-24 hours dwell at room temperature (e.g., 20-25°C), the bonded panel was clamped 2° from vertical in an oven maintained at 70°C with a 500 gram weight attached to the free end ofthe composite. The time to failure was determined in minutes and was the average value of three replicates unless otherwise noted. If failure did not occur by 10,000 minutes, the test was discontinued.
- a 0.25 mm thick layer of pressure sensitive adhesive prepared generally according to Example 10 in U.S. Patent No. 5,342,685 was coated onto a two-sided silicone-coated release paper liner.
- the adhesive-coated release liner was hand laminated to a 0.1 mm extruded clear low density polyethylene film prepared from PETROTHENE NA 964-085 resin obtained from Quantum Chemical Corp., Cincinnati, Ohio (backing strip 2 in Table 1).
- the coated film was cut into 2.5 cm x 2.5 cm squares.
- the adhesive composition included 19.8 wt-% KRATON 1118 mbber available from Shell Chemical Co., Houston, Texas, 20.8 wt-% SOLPRENE 1205 rubber, available from Housemex, Inc., Houston, Texas, 48.3 wt-% PICCOLYTE A135 resin, available from Hercules, Inc., Brunswick, Georgia, 10.1 wt-% SHELLFLEX 371 oil, available from Shell Chemical Co., Houston, Texas, and 1.0 wt-% IRGANOX 1076 antioxidant, available from Ciba Geigy, Mclntosh, Texas.
- the patch was applied as a field repair to a 700 mm x 25 mm diameter touring bicycle inner tube to a puncture having an approximate size of
- the tube was roughened with sandpaper before applying the patch using hand pressure.
- the inner tube was inserted in the tire and was inflated to about 690 kilopascals. The patch has not failed during 3 months of use.
- a test device was constmcted to compare bond strength of pressure sensitive patches to inner tube surfaces while in an air expanded mode.
- This device had a 3.8 cm deep x 10.2 cm diameter cavity machined into a 5.1 cm deep x 15.2 cm diameter aluminum cylinder.
- a 0.32 cm thick aluminum ring of 10.2 cm inside diameter and 15.2 cm outside diameter dimension was used as a retaining ring to hold 12.7 cm diameter mbber inner tube samples.
- An air inlet tube with an open/close valve and air gauge was attached to a hole in the wall which allowed air to be injected into and held in the cylinder.
- Four patches were compared using this fixture. The purpose was to determine the patch's ability to seal air in the cylinder after pressurization. The patches are described as follows:
- a 12.7 cm diameter disc was cut from an inner tube.
- Four punctures were made in the mbber disc with a 1.14 mm diameter pin.
- Surface preparation ofthe puncture area was accomplished according to the instmctions contained in each commercial package.
- Patches #1, 2, and 4 required abrading the punctured area with an abrasion material provided with each package of patches.
- Patch #3 required cleaning the puncture area with an alcohol prep pad provided with the patch package.
- a patch of each type was placed over one ofthe four punctures.
- An applied static pressure of 23 kg was placed on each patch area for 15 seconds using a hand operated pressure applicator with a Chatillon force gauge.
- the mbber disc was clamped between the open end ofthe aluminum vessel and the 3.18 mm thick aluminum washer shaped top ring.
- the sealed device was then slowly inflated to about 55 kPa. This pressure caused the mbber disc to balloon and form a shape similar to about 80% of a sphere.
- the inflated device was submerged in water to detect air leakage and the following was observed: Patch #3 failed immediately.
- the PSA bonded better to the butyl mbber tube material than to the mbber patch.
- patches #1 and #4 did not fail; however, air pressure drop caused by failures of patches 2 and 3 curtailed the test.
- patch #4 failed immediately as the PSA lifted from the tube surface.
- failure occurred as a result of air escaping along the channels and cuts made by abrading the surface ofthe tube with too much pressure. The PSA did not fail or lift from the surface, however.
- a fourth test of patch #1 on a puncture area that had been cleaned by wiping with a dry cloth did not fail. Three other patches were tested using this fixture. The patches are described as follows:
- Example 2 A 0.25 mm thick layer of pressure sensitive adhesive from Example 2 was laminated to a non-stretchable 0.051 mm thick primed polyester film backing. A 25.4 mm x 25.4 mm square sample with rounded comers was cut out. The sample was tested the same as Example 3. The sample adhered to the mbber, but started to peel around the edges within 10 minutes of inflation at 55 kPa. This example represents the importance of using an elastic backing in an unconstrained application.
- Example 3 A non-stretchable 25.4 mm x 25.4 mm square sample of 3M SCOTCH brand transparent film tape #622 with rounded comers was tested the same as Example 3. The sample started to fail within the first minute of inflation by peeling around the edges, and failed completely within 8 minutes.
- Example 3 The adhesive patch adhered very well to the vinyl film. The patch performed for 24 hours at a pressure of 55 kPa without failing.
- the tackified acrylate adhesive was prepared as follows: A composition was prepared by mixing 82 parts isooctyl acrylate (IOA), 17 parts isobornyl acrylate (IB A), 1 part acrylic acid (AA), and 0.04 pph benzil dimethyl ketal photoinitiator (EscacureTMKB-l available from Sartomer Co.) in a closed glass container.
- IOA isooctyl acrylate
- IB A isobornyl acrylate
- AA acrylic acid
- EscacureTMKB-l available from Sartomer Co.
- the container was purged with nitrogen, and as the nitrogen purging continued, the composition was irradiated with an ultraviolet black light (GE F15T8 BL from General Electric Co.) which was partially taped with black tape to provide an intensity of about 0.15 milliwatts per square centimeter (mW/cm 2 ), measured according to the industry standard G unit, to form a symp having a coatable viscosity estimated to be about 3000 centipoise.
- an ultraviolet black light GE F15T8 BL from General Electric Co.
- the mixture was knife coated to a thickness of about 0.25 mm onto a paper release liner that had been coated with a silicone release coating, and then exposed to fluorescent black lamps in a nitrogen rich atmosphere (50-100 ppm oxygen) for 5 minutes to form a pressure-sensitive adhesive transfer tape.
- the intensity was 1.7 milliWatts/square centimeter (mW/cm 2 ) for 1.7 minutes and 4.2 mW/cm 2 for 3.3 minutes, measured according to the National Institute Standards units (NIST units).
- the fluorescent black lamps had about 90% of their emission spectra between about 300 and 400 nanometers (nm), with a peak emission at about 350 nm.
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Abstract
Description
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MX9800683A MX9800683A (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch. |
US08/495,426 US5643648A (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch |
CA002227525A CA2227525A1 (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch |
PCT/US1995/009467 WO1997004947A1 (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch |
AU31501/95A AU3150195A (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US1995/009467 WO1997004947A1 (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997004947A1 true WO1997004947A1 (en) | 1997-02-13 |
Family
ID=22249527
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/009467 WO1997004947A1 (en) | 1995-07-26 | 1995-07-26 | Pressure sensitive adhesive patch |
Country Status (5)
Country | Link |
---|---|
US (1) | US5643648A (en) |
AU (1) | AU3150195A (en) |
CA (1) | CA2227525A1 (en) |
MX (1) | MX9800683A (en) |
WO (1) | WO1997004947A1 (en) |
Cited By (1)
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WO2007011539A3 (en) * | 2005-07-15 | 2007-03-22 | 3M Innovative Properties Co | Automobile panel repair laminate |
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US5894864A (en) * | 1995-07-26 | 1999-04-20 | Rich; Benjamin P. | Repair or maintenance system for leaking pipes or pipe joints |
US5822857A (en) * | 1996-03-18 | 1998-10-20 | Ngk Insulators, Ltd. | Method of repairing shed portion of composite insulator |
DE10243441B4 (en) * | 2002-09-18 | 2004-12-30 | Continental Aktiengesellschaft | Tire transponder |
US20050187085A1 (en) * | 2004-02-24 | 2005-08-25 | Webb Nicholas J. | Inflatable abdominal exercise apparatus |
US20050250630A1 (en) * | 2004-05-10 | 2005-11-10 | Webb Nicholas J | Inflatable abdominal exercise apparatus |
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US20080116684A1 (en) * | 2006-11-16 | 2008-05-22 | Datacard Corporation | Mini patch laminate |
US20090236256A1 (en) * | 2008-03-21 | 2009-09-24 | Shinnick Douglas W | Patch for damaged bags |
US8765217B2 (en) | 2008-11-04 | 2014-07-01 | Entrotech, Inc. | Method for continuous production of (meth)acrylate syrup and adhesives therefrom |
US8329079B2 (en) | 2009-04-20 | 2012-12-11 | Entrochem, Inc. | Method and apparatus for continuous production of partially polymerized compositions and polymers therefrom |
US20110030255A1 (en) * | 2009-08-10 | 2011-02-10 | Morris Eric C | Inflatable sign and kit |
DE102009050899A1 (en) * | 2009-10-27 | 2011-04-28 | Rema Tip Top Gmbh | Repair plaster for an elastomeric component, in particular for a vehicle tire, with increased adhesive strength |
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WO2012119227A1 (en) | 2011-03-04 | 2012-09-13 | Surface Medical Inc. | Adhesive patch and method of using the same |
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US9279701B2 (en) | 2014-01-27 | 2016-03-08 | Basic Electronics, Inc. | Method and system for reading utility meters |
US10807120B2 (en) * | 2015-08-24 | 2020-10-20 | Rubberlite, Inc. | Foam tape |
US11458698B2 (en) | 2020-11-23 | 2022-10-04 | Pb&Jj, Llc | Inflatable device repair kit |
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- 1995-07-26 US US08/495,426 patent/US5643648A/en not_active Expired - Fee Related
- 1995-07-26 MX MX9800683A patent/MX9800683A/en unknown
- 1995-07-26 CA CA002227525A patent/CA2227525A1/en not_active Abandoned
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007011539A3 (en) * | 2005-07-15 | 2007-03-22 | 3M Innovative Properties Co | Automobile panel repair laminate |
AU2006270420B2 (en) * | 2005-07-15 | 2011-02-24 | 3M Innovative Properties Company | Automobile panel repair laminate |
US8353995B2 (en) | 2005-07-15 | 2013-01-15 | 3M Innovative Properties Company | Automobile panel repair laminate |
Also Published As
Publication number | Publication date |
---|---|
MX9800683A (en) | 1998-04-30 |
US5643648A (en) | 1997-07-01 |
CA2227525A1 (en) | 1997-02-13 |
AU3150195A (en) | 1997-02-26 |
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